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一名肾移植患者患棘状毛发发育异常症。

Trichodysplasia spinulosa in a renal transplant patient.

作者信息

Laroche Alexandre, Allard Catherine, Chababi-Atallah Myrna, Masse Mélanie, Bertrand Janie

机构信息

Faculté de Médecine et des Sciences de la SantéDepartment of Microbiology and Infectiology, CHU SherbrookeDepartment of Pathology, CHU SherbrookeDepartment of Medicine, Service of Nephrology, CHU SherbrookeDepartment of Medicine, Service of Dermatology, CHU Sherbrooke, Université de Sherbrooke, Sherbrooke, QC

Faculté de Médecine et des Sciences de la SantéDepartment of Microbiology and Infectiology, CHU SherbrookeDepartment of Pathology, CHU SherbrookeDepartment of Medicine, Service of Nephrology, CHU SherbrookeDepartment of Medicine, Service of Dermatology, CHU Sherbrooke, Université de Sherbrooke, Sherbrooke, QC.

出版信息

J Cutan Med Surg. 2015 Jan-Feb;19(1):66-8. doi: 10.2310/7750.2014.13174. Epub 2015 Jan 1.

DOI:10.2310/7750.2014.13174
PMID:25775666
Abstract

BACKGROUND

Trichodysplasia spinulosa (TS) is a rare skin affection seen in immunocompromised patients, mainly those with solid organ tranplants.

OBJECTIVE

To report a case of a patient with classic clinical and pathologic findings for the disease so that physicians caring for this population are aware of the clinical presentation.

METHOD

We report the case of a female patient we saw at our clinic with a diagnosis of TS.

RESULTS

The diagnosis of TS was confirmed by pathologic findings.

CONCLUSION

TS should be considered in any immunocompromised patient with a papular facial eruption reminiscent of acne vulgaris and with keratotic spiny papules as a distinctive feature.

摘要

背景

棘状毛发发育异常(TS)是一种在免疫功能低下患者中出现的罕见皮肤疾病,主要见于实体器官移植患者。

目的

报告一例具有该疾病典型临床和病理表现的患者,以便治疗这类患者的医生了解其临床表现。

方法

我们报告在我们诊所诊断为TS的一名女性患者的病例。

结果

病理结果证实为TS。

结论

对于任何免疫功能低下且面部出现丘疹性皮疹、类似寻常痤疮并伴有角化性棘状丘疹这一独特特征的患者,都应考虑TS的可能。

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J Eur Acad Dermatol Venereol. 2021 May;35(5):1067-1076. doi: 10.1111/jdv.17081. Epub 2021 Jan 6.
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Photodynamic therapy for the treatment of trichodysplasia spinulosa in an Asian renal transplant recipient: A case report and review of literature.
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